A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994506



Internal ID21903849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9217681..9226391hg38UCSC Ensembl
chr3:9259365..9268075hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg388711
hg198711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533044
Samples
Known GenesSRGAP3, SRGAP3-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994506
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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